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3-(dimethylamino)-1-[4-(hydroxymethyl)-1,3-thiazol-2-yl]prop-2-en-1-one | 774230-92-1

中文名称
——
中文别名
——
英文名称
3-(dimethylamino)-1-[4-(hydroxymethyl)-1,3-thiazol-2-yl]prop-2-en-1-one
英文别名
——
3-(dimethylamino)-1-[4-(hydroxymethyl)-1,3-thiazol-2-yl]prop-2-en-1-one化学式
CAS
774230-92-1
化学式
C9H12N2O2S
mdl
——
分子量
212.272
InChiKey
MAENZKVALPVRLK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    81.7
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    N-(3-hydroxy-5-trifluoromethyl-phenyl)-guanidine 、 3-(dimethylamino)-1-[4-(hydroxymethyl)-1,3-thiazol-2-yl]prop-2-en-1-onepotassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 生成 C15H11F3N4O2S
    参考文献:
    名称:
    Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)
    摘要:
    A series of SYK inhibitors based on the phenylamino pyrimidine thiazole lead 4 were prepared and evaluated for biological activity. Lead optimization provided compounds with nanomolar K(i)'s against SYK and potent inhibition in mast cell degranulation assays.
    DOI:
    10.1016/j.bmcl.2008.09.106
  • 作为产物:
    参考文献:
    名称:
    Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)
    摘要:
    A series of SYK inhibitors based on the phenylamino pyrimidine thiazole lead 4 were prepared and evaluated for biological activity. Lead optimization provided compounds with nanomolar K(i)'s against SYK and potent inhibition in mast cell degranulation assays.
    DOI:
    10.1016/j.bmcl.2008.09.106
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文献信息

  • Thiazoles useful as inhibitors of protein kinases
    申请人:Brenchley Guy
    公开号:US20050004150A1
    公开(公告)日:2005-01-06
    The present invention relates to compounds useful of inhibitors of protein kinases. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.
    本发明涉及一种有用的蛋白激酶抑制剂化合物。本发明还提供了包含该化合物的药学上可接受的组合物,并提供了使用该组合物治疗各种疾病、病况或障碍的方法。
  • US7276502B2
    申请人:——
    公开号:US7276502B2
    公开(公告)日:2007-10-02
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